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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Functional & integrative genomics 1 (2000), S. 2-11 
    ISSN: 1438-7948
    Keywords: Arabidopsis Genome sequencing Gene traps Redundancy Genome mapping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The Arabidopsis genome sequence is scheduled for completion at the end of this year (December 2000). It will be the first higher plant genome to be sequenced, and will allow a detailed comparison with bacterial, yeast and animal genomes. Already, two of the five chromosomes have been sequenced, and we have had our first glimpse of higher eukaryotic centromeres, and the structure of heterochromatin. The implications for understanding plant gene function, genome structure and genome organization are profound. In this review, the lessons learned for future genome projects are reviewed as well as a summary of the initial findings in Arabidopsis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 191 (1983), S. 182-188 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Five different DNA insertions (ISH1, ISH2, ISH23, ISH24, and ISH25) are found in or upstream of the bacterio-opsin (bop) gene in Bop mutants of H. halobium. These insertions have been cloned and characterized. They range in size from 520–3,000 bp, and four of the five insertions have structural features similar to known transposable elements. Two of the elements (ISH1 and ISH2) are found in the majority of Bop mutants. The former integrates at a preferred target site, while the latter integrates at numerous sites. The copy number of each insertion element was determined along with its distribution in the 68% G+C (FI), 58% G+C (FII) and cccDNA fractions of the H. halobium genome. There are eight copies of ISH2, one copy in FI and seven in the cccDNA. There are two copies of each of the other three insertion elements and one copy of ISH25. ISH25 does not seem to have the usual structural features of a transposable element. Most of the copies of these insertion elements are located in the cccDNA. Vacuole, ruberin and purple membrane mutants of H. halobium occur at high spontaneous frequencies. Rearrangements, insertions and deletions occur concurrently in the FII and cccDNA of these mutants including insertions of these five elements. Although the bacterio-opsin gene incurs insertions frequently, the 40 kb of flanking FI DNA remains conserved in mutant derivatives of H. halobium and in a number of related species.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 209 (1987), S. 33-40 
    ISSN: 1617-4623
    Keywords: Wheat chromosome 5 ; Grain development ; Germination ; Intron evolution ; Upstream regulatory sequences
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A genomic clone of a wheat α-amylase gene (λAmy3/33) was identified, on the basis of hybridisation properties, as different from α-Amy1 and α-Amy2 genes which had been characterised previously. The nucleotide sequence revealed that this gene has the normal sequence motifs of an active gene and an open reading frame interrupted by two introns. The protein sequence encoded by this open reading frame is recognisably similar to that of α-amylase from the α-Amy1 and α-Amy2 genes and there is high sequence homology in all three proteins at the putative active sites and Ca++ binding region. In addition, the introns are at positions equivalent to the position of introns in the α-Amy1 and α-Amy2 genes. However, the sequence was less similar to α-Amy1 and α-Amy2 than these are to each other. Southern blot analysis showed that the λAmy3/33 DNA is one of a small multigene family carried on a different chromosome (group 5) from either the α-Amy1 or α-Amy2 genes. A further difference from the α-Amy1 and α-Amy2 genes was the pattern of expression. λAmy3/33 was expressed only in immature grains and, unlike the α-Amy1 and α-Amy2 genes, not at all in germinating aleurones. These data suggested therefore that this gene represents a third type of α-amylase gene, not described before, which shares a common evolutionary ancestor with the α-Amy1 and α-Amy2 genes.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 214 (1988), S. 232-240 
    ISSN: 1617-4623
    Keywords: α-Amylase ; Chromosome location ; Promoter sequence comparisons ; Sequence heterogeneity ; Tissuespecific expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The α-Amy2 genes of wheat are a multigene family which is expressed in the aleurone cells of germinating grain under control of the plant hormone gibberellin. A subset of the genes are also expressed in developing grain. Comparison of five genomic clones containing α-Amy2 genes, using DNA sequence analysis and Southern hybridisation, showed that the extent of similarity between genes differed. Two of the most heterogeneous genes compared were located to the same group 7 chromosome while the most similar genes α-Amy2/54 and α-Amy2/8 were located to different ones; hence sequence variation could not be correlated to the ancestry of the α-Amy2 genes during the separate existence of the constituent genomes of hexaploid wheat. Expression of the cloned genes was measured using an S1 nuclease protection assay and this identified α-Amy2/54 and α-Amy2/8 as part of the subset of α-Amy2 genes expressed in both the developing grain and in aleurone cells. Comparison of the 5′ upstream regions of all five genes showed high similarity, with the exception of one gene, up to-280 nucleotides from the transcriptional start, while similarity between α-Amy2/54 and α-Amy2/8 extended a further 90 bp upstream of this point. It is suggested that regulatory elements responsible for tissue specificity and gibberellin regulation may be located within these regions of similarity.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1617-4623
    Keywords: Transposons ; Multigene family ; Repeated DNA sequences ; Restriction fragment length polymorphism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Comparison of the 5′ flanking regions of three α-amylase genes from chromosome 6B of hexaploid wheat by heteroduplex and sequence analysis revealed the presence of a 1.6 kb stem-loop insertion sequence (WIS1) in one of them. Polymorphism among hexaploid wheat varieties suggests the relatively recent insertion/excision of this sequence from its present position. The complete sequence of the stem-loop insertion shows that it has many of the features found in transposable elements, including target site duplication and terminal inverted repeats. One unusual feature is a tandem array of direct repeats comprising a wheat “minisatellite” sequence. Both the insertion sequence and the minisatellite are found at multiple locations in the wheat genome, but the functional significance of their association in WIS1 is unknown. The minisatellite arrays share a common core structure, and long arrays are polymorphic between different hexaploid varieties.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Plant molecular biology 5 (1985), S. 13-24 
    ISSN: 1573-5028
    Keywords: α-amylase ; gene ; gibberellic acid ; mRNA ; multigene family
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The α-Amy1 and α-Amy2 genes of wheat produce distinct subsets of α-amylase isozymes which show different patterns of expression in wheat aleurone cells and in developing grain. In order to characterise the organisation and expression of these genes, clones of α-Amy1 and α-Amy2 cDNA have been isolated. The two types of cDNA clone were distinguished within a small library of α-amylase cDNA clones (Baulcombe and Buffard, Planta 157 493–501 [1983]) by restriction endonuclease mapping and by cross hybridisation. The identity of α-Amy1 or α-Amy2 type was assigned from the results of hybrid selected translation analysis in which small subfragments of the cDNA clones were used. These subfragments were derived from the 3′ ends of the cDNA and did not cross hybridise between the different types of cDNA. Hybridisation of α-Amy1 and α-Amy2 cDNA probes to restriction enzyme digests of wheat nuclear DNA revealed that these are multigene families located on the group 6 (α-Amy1) and group 7 (α-Amy2) chromosomes. Studies on the levels of α-Amy1 and α-Amy2 mRNA in developing grain and in aleurone tissue indicated that the differences in isozyme expression are due to the patterns of mRNA accumulation. In aleurone tissue the α-Amy1 transcripts accumulate in parallel with other genes which are regulated by gibberellic acid, while the accumulation of α-Amy2 genes is sustained for 36 h longer.
    Type of Medium: Electronic Resource
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